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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072209Generated: November 1, 2026

Ammonia → HCID 13273295, compound

https://huagongshe.com/reaction/2072209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantChloroformHCID 6212—
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 13273294HCID 13273294—
SolventTriethylamineHCID 8471—
ProductHCID 13273295HCID 13273295—

Reaction Steps

To a solution of 0.258 g. of 1-[2-(2-pyridinecarbonyl)phenyl]-5-chloromethyl-1H-1,2,4-triazole-3-carboxylic acid in 7.5 ml. of chloroform are added 0.14 ml. of triethylamine and then 0.1 ml. of ethyl chlorocarbonate with ice-cooling. After stirring for 10 minutes, to the resulting mixture is added 0.5 ml. of concentrated aqueous ammonia, and the whole mixture is further stirred for 30 minutes. The precipitated crystals are collected by filtration, washed successively with water, ethanol and ether, and then dried to give 1-[2-(2-pyridinecarbonyl)phenyl]-5-chloromethyl-1H-1,2,4-triazole-3-carboxamide as crystals. The filtrate is extracted with chloroform and the chloroform layer is washed with water, dried over sodium sulfate, followed by evaporation of the solvent to give additional crystals identical with the abovementioned crystals. Recrystallization of the combined crystals from chloroform-ethanol gives colorless needles, melting at 228° to 229° C. (decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04049812
Source datasetuspto-grants-1977_09
ORD IDord-6da33c2c11b4443db8ee4fff1550dea3
Source noteuspto-grants-1977_09